# FDA Inspection 1074202 - Neal S. Kleiman, M.D. - December 06, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/neal-s-kleiman-md/6e7f99b8-b8f2-448f-8a8f-7fa8d00dd62e
Source feed: FDA_Inspections

> FDA Inspection 1074202 for Neal S. Kleiman, M.D. on December 06, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1074202
- Company Name: Neal S. Kleiman, M.D.
- Inspection Date: 2018-12-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 856696 - 2013-11-26](https://www.globalkeysolutions.net/records/fda_inspections/neal-s-kleiman-md/e4c22842-c6e7-49fd-acd6-746aa6e73a71)

Company: https://www.globalkeysolutions.net/companies/neal-s-kleiman-md/276044d0-46fe-45c7-9b31-acaaa7ed1423

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7